Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2737-2020 — Progressa Bed, Catalog No. P7500 - Product Usage: intended to be used to treat or prevent pulmonary or other complications associated with immobility; to treat or prevent pressure ulcers; or for any other use where medical benefits may be derived from either Continuous Lateral Rotation Therapy or Pe

U.S. FDA — Device Enforcement · United States · 2020-06-30 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2737-2020
Date of alert: 2020-06-30
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Hill-Rom, Inc.
Product category: device
Product type: Devices

Reported risk: Affected beds may have screws installed that do not meet material tensile strength requirements. Failure of this screw could result in serious patient or user injury.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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